Medtronic In.Pact Admiral Catheter recall in Canada: infection risk
In plain language
This recall involves the Medtronic In.Pact Admiral Paclitaxel-coated PTA Balloon Catheter sold in Canada. It's being recalled because damage to the sterile pouch could lead to a loss of sterility and potential infection. Contact the manufacturer for more information if you have this product.
What to do
- Contact the manufacturer if you require additional information.
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Affected products
In.Pact Admiral Paclitaxelcoated Pta Balloon Catheter
Lot: ADM07006013P, ADM05004013P, ADM06008013P, ADM04015013P, ADM06004013P, ADM05008013P, ADM06015013P
Why this matters
Infection risk due to loss of sterility
Do I have this product?
This recall only applies to specific products. Follow the steps below to check.
- 1
Check the product name
Make sure your product name matches one of the affected products listed above.
- 2
Check the lot number
Lot numbers identify specific production batches.
Affected lots: ADM07006013P, ADM05004013P, ADM06008013P, ADM04015013P, ADM06004013P, ADM05008013P, ADM06015013P
If your product matches one or more of the details above, it may be affected by this recall.
If your product does not match these details, it is not affected by this recall.
When in doubt, always check the official notice.
Frequently Asked Questions
Why was this product recalled?
Infection risk due to loss of sterility
What should consumers do?
Contact the manufacturer if you require additional information.
Where was the product sold?
This product was sold in Canada. For specific retailers or distribution areas, please check the official recall notice linked on this page.
Is there a health risk?
Yes, there may be a health risk. Infection risk due to loss of sterility
When was this product recalled?
This product was recalled on April 4, 2022.
Is the MEDTRONIC INC. brand affected by this recall?
Yes, MEDTRONIC INC. products are affected by this recall. This recall involves the Medtronic In.Pact Admiral Paclitaxel-coated PTA Balloon Catheter sold in Canada. It's being recalled because damage to the sterile pouch could lead to a loss of sterility and potential infection. Contact the manufacturer for more information if you have this product.